MOF-Derived Hollow C, N-Doped Co3O4 Dodecahedral Nanostructure Enwrapped with MgIn2S4 Nanosheets for Enhanced Photocatalytic N2 Reduction

被引:2
|
作者
Bariki, Ranjit [1 ]
Sahoo, Sudhir K. [2 ]
Pati, Aditya Ranjan [1 ]
Pradhan, Sibun Kumar [1 ]
Panda, Saumyaranjan [1 ]
Nayak, Swagat Kumar [1 ]
Mishra, Braja Gopal [1 ]
机构
[1] Department of Chemistry, National Institute of Technology, Odisha, Rourkela,769008, India
[2] Department of Chemistry, Indian Institute of Technology, Karnataka, Dharwad,580007, India
关键词
Carbonization - Catalytic cracking - Defect density - Low temperature production - Photocatalytic activity - Quality assurance - Semiconductor doping;
D O I
10.1021/acs.inorgchem.4c04746
中图分类号
学科分类号
摘要
Design of hierarchical hollow nanoheterostructure materials through interfacial and defect engineering is an innovative approach for achieving optimal charge separation dynamics and photon harvesting efficiency. Herein, we have described a facile technique to fabricate hollow MOF-derived C, N-doped-Co3O4 (C, N-Co3O4) dodecahedral particles enwrapped with MgIn2S4 nanosheets for enhanced N2 reduction performance. ZIF-67 was initially used as a sacrificial template to prepare hollow C, N-Co3O4 using a carbonization route followed by low-temperature calcination treatment. The controlled synthetic protocol not only led to nonmetal doping but also produced an interwoven carbon matrix that improved the photoelectron mobility. Density functional theory calculations further substantiated the creation of atomic defects through substitution of C at tetrahedral Co2+ sites and N at lattice O2- sites of the Co3O4 structure. C, N-Co3O4 was subsequently coupled with MgIn2S4 nanosheets to prepare the C, N-Co3O4/MgIn2S4 [C, N-CM (X)] p-n heterojunctions. The photocatalytic study revealed that the NH4+ ion production activity of the optimal C, N-CM (1:1) material (334 μmol g-1 h-1) was significantly higher (4-10 times) than that of pure components. The enhanced activity of the composite was ascribed to its distinct topological features, superior charge carrier dynamics, and creation of atomic defects that afforded a large number of surface-active sites. © 2024 American Chemical Society.
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页码:412 / 426
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